Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178406
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Numbers/UDI 018050 (01)00880304259744(17)270807(10)018050; 018050R (01)00880304259744(17)270807(10)018050R; 056160 (01)00880304259744(17)270108(10)056160; 332030 (01)00880304259744(17)270702(10)332030; 332050 (01)00880304259744(17)270710(10)332050; 608510 (01)00880304259744(17)270924(10)608510; 608600 (01)00880304259744(17)271026(10)608600; 671730 (01)00880304259744(17)270831(10)671730; 752780 (01)00880304259744(17)270817(10)752780;
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Biomet, Inc.
- Reason for Recall:
- Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178406
Product Codes/Lot Numbers:
Lot Numbers/UDI 018050 (01)00880304259744(17)270807(10)018050; 018050R (01)00880304259744(17)270807(10)018050R; 056160 (01)00880304259744(17)270108(10)056160; 332030 (01)00880304259744(17)270702(10)332030; 332050 (01)00880304259744(17)270710(10)332050; 608510 (01)00880304259744(17)270924(10)608510; 608600 (01)00880304259744(17)271026(10)608600; 671730 (01)00880304259744(17)270831(10)671730; 752780 (01)00880304259744(17)270817(10)752780;
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0373-2024
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